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Infection and Immunity, December 1998, p. 5777-5784, Vol. 66, No. 12
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Pseudomonas Pyocyanin Increases
Interleukin-8 Expression by Human Airway Epithelial Cells
Gerene M.
Denning,1,*
Laura A.
Wollenweber,1
Michelle A.
Railsback,1
Charles D.
Cox,2
Lynn L.
Stoll,1 and
Bradley E.
Britigan1
Departments of Internal
Medicine1 and
Microbiology,2 The VA Medical Center and The
University of Iowa, Iowa City, Iowa 52242
Received 30 March 1998/Returned for modification 20 May
1998/Accepted 2 September 1998
Pseudomonas aeruginosa, an opportunistic human
pathogen, causes acute pneumonia in patients with hospital-acquired
infections and is commonly associated with chronic lung disease in
individuals with cystic fibrosis (CF). Evidence suggests that the
pathophysiological effects of P. aeruginosa are mediated in
part by virulence factors secreted by the bacterium. Among these
factors is pyocyanin, a redox active compound that increases
intracellular oxidant stress. We find that pyocyanin increases release
of interleukin-8 (IL-8) by both normal and CF airway epithelial cell
lines and by primary airway epithelial cells. Moreover, pyocyanin
synergizes with the inflammatory cytokines tumor necrosis factor alpha
and IL-1
. RNase protection assays indicate that increased IL-8
release is accompanied by increased levels of IL-8 mRNA. The
antioxidant n-acetyl cysteine, general inhibitors of
protein tyrosine kinases, and specific inhibitors of mitogen-activated
protein kinases diminish pyocyanin-dependent increases in IL-8 release.
Conversely, inhibitors of protein kinases C (PKC) and PKA have no
effect. In contrast to its effects on IL-8 expression, pyocyanin
inhibits cytokine-dependent expression of the
monocyte/macrophage/T-cell chemokine RANTES. Increased release of IL-8,
a potent neutrophil chemoattractant, in response to pyocyanin could
contribute to the marked infiltration of neutrophils and subsequent
neutrophil-mediated tissue damage that are observed in
Pseudomonas-associated lung disease.
*
Corresponding author. Mailing address: Building 3, Room
139, VA Medical Center, Iowa City, IA 52246. Phone: (319) 338-0581, ext. 7573. Fax: (319) 339-7162. E-mail:
gerene-denning{at}uiowa.edu.
Infection and Immunity, December 1998, p. 5777-5784, Vol. 66, No. 12
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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